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METHYL 4-AMINO-3-NITROBENZOATE

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METHYL 4-AMINO-3-NITROBENZOATE Basic information

Product Name:
METHYL 4-AMINO-3-NITROBENZOATE
Synonyms:
  • 4-AMINO-3-NITROMETHYLBENZOATE
  • 3-Nitro-4-aminobenzoic acid methyl ester
  • 4-Amino-3-nitrobenzoic acid methyl ester
  • METHYL 4-AMINO-3-NITROBENZENECARBOXYLATE
  • METHYL 4-AMINO-3-NITROBENZOATE
  • methyl 4-amino-3-nitrobenzoatemethyl 4-amino-3-nitrobenzoate
  • Methyl 3-nitro-4-aminobenzoate
  • 2-Amino-5-(methoxycarbonyl)nitrobenzene, 4-(Methoxycarbonyl)-2-nitroaniline
CAS:
3987-92-6
MF:
C8H8N2O4
MW:
196.16
Product Categories:
  • Aromatic Esters
Mol File:
3987-92-6.mol
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METHYL 4-AMINO-3-NITROBENZOATE Chemical Properties

Melting point:
204-206°C
Boiling point:
392.8±22.0 °C(Predicted)
Density 
1.386±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
-2.59±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2922390090
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METHYL 4-AMINO-3-NITROBENZOATE Usage And Synthesis

Chemical Properties

Methyl 4-amino-3-nitrobenzoate is a synthetic compound that has been found to have a variety of uses. It has been used to prepare intramolecular hydrogen bonds in anilines, and it can be used as an intermediate to synthesize amides and anilines. This molecule also forms resonance structures with the nitro group, which allows for increased stability. The proton magnetic resonance spectra of Methyl 4-amino-3-nitrobenzoate show that the molecule has a high degree of symmetry, which is due to the presence of intramolecular hydrogen bonding.

Synthesis

67-56-1

1588-83-6

3987-92-6

4-Amino-3-nitrobenzoic acid (50 g, 270 mmol, 1 eq.) was suspended in methanol (600 mL) at room temperature. Subsequently, sulfoxide chloride (20 mL, 270 mmol, 1 eq.) was slowly added dropwise to the above suspension. The reaction mixture was heated to reflux for 16 h. After completion of the reaction, it was cooled to room temperature. The resulting yellow solid, methyl 4-amino-3-nitrobenzoate (D1) (53 g, 100% yield), was collected by filtration, and the product could be used in subsequent reactions without further purification. Mass spectrometry analysis showed [M + H]+ = 197.3, retention time (RT) = 2.42 min.

References

[1] Patent: WO2004/94430, 2004, A1. Location in patent: Page 16
[2] Patent: WO2006/40148, 2006, A1. Location in patent: Page/Page column 19-20
[3] Patent: WO2015/57938, 2015, A1. Location in patent: Page/Page column 102
[4] Patent: CN106146416, 2016, A. Location in patent: Paragraph 0046; 0047; 0048; 0049; 0050
[5] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 8 - 20

METHYL 4-AMINO-3-NITROBENZOATESupplier

Alfa Aesar
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Jia Xing Isenchem Co.,Ltd
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Adamas Reagent, Ltd.
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